Allele Registry

Canonical Allele Identifier: PA192027

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000164891

RCV000200231

RCV000480270

RCV000524126

RCV000781602

RCV001094683

RCV003462152

RCV004528912

ClinVar Variation:

185463

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu639Lys	CA009445 NM_000179.3:c.1915G>A